US4350700A - Pharmaceutical composition containing 1,3,5-substituted biuret compound - Google Patents
Pharmaceutical composition containing 1,3,5-substituted biuret compound Download PDFInfo
- Publication number
- US4350700A US4350700A US06/257,583 US25758381A US4350700A US 4350700 A US4350700 A US 4350700A US 25758381 A US25758381 A US 25758381A US 4350700 A US4350700 A US 4350700A
- Authority
- US
- United States
- Prior art keywords
- group
- sub
- substituted
- methyl
- lower alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/40—Acylated substituent nitrogen atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/17—Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C273/00—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C273/18—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas
- C07C273/1854—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas by reactions not involving the formation of the N-C(O)-N- moiety
- C07C273/1863—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas by reactions not involving the formation of the N-C(O)-N- moiety from urea
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C273/00—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C273/18—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas
- C07C273/1872—Preparation of compounds comprising a -N-C(O)-N-C(O)-N- moiety
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/38—Nitrogen atoms
- C07D277/44—Acylated amino or imino radicals
- C07D277/48—Acylated amino or imino radicals by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof, e.g. carbonylguanidines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/62—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to atoms of the carbocyclic ring
- C07D317/66—Nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/30—Hetero atoms other than halogen
- C07D333/36—Nitrogen atoms
Definitions
- the present invention relates to a pharmaceutical composition containing a 1,3,5-substituted biuret compound. More particularly, the present invention relates to an analgesic, anti-inflammatory or anti-pyretic composition containing as the active ingredient 1,3,5-substituted biuret compound of the formula (1), ##STR2## wherein R 1 is a hydrogen atom, a lower alkyl group, a substituted lower alkyl group having chlorine atom(s), cyano group(s), dimethylamino group(s), hydroxy group(s), methoxy group(s) or carboxy group(s) as the substituent(s), a lower alkenyl group, a hydroxy group, a methoxy group, an acetyl group or a phenyl group; R 2 is a hydrogen atom, a lower alkyl group or a phenyl group; R 3 is a phenyl group, a substituted phenyl group having halogen atom(s), trifluor
- the object of the present invention is to provide novel 1,3,5-substituted biuret compounds.
- Another object of the present invention is to provide an analgesic, anti-inflammatory or anti-pyretic composition containing 1,3,5-substituted biuret compound as the active ingredient.
- the 1,3,5-substituted biuret compound of the formula (1) can be prepared by any processes shown below.
- the reaction of the urea with the isocyanate may be carried out in the presence or absence of a solvent.
- the solvent used in this reaction is not subjected to any specific restriction and any known inert type which gives no adverse effect to the reaction can be used.
- the solvents are ethers such as ether, dioxane, tetrahydrofuran and the like; halogenated lower alkanes such as methylene chloride, chloroform, carbon tetrachloride and the like; aromatic hydrocarbons such as benzene, toluene, xylene and the like.
- the ratio of amount of the urea and the isocyanate in this reaction is not subjected to any specific restriction and may be suitably selected from a wide range, and usually, it is desirable that they are used in equimolar quantity respectively.
- the reaction temperature is also not subjected to any particular restriction and may be suitably selected from a wide range, and usually the reaction can advantageously be carried out at a room temperature to the boiling point of the solvent used generally within the range of 20° to 200° C.
- the obtained 1,3,5-substituted biuret compound of the formula (1) can be isolated by usual separation means.
- the reaction of the allophanoyl chloride with the amine may be carried out in a solvent.
- the solvent used in this reaction is not subjected to any specific restriction and any known inert type which gives no adverse effect to the reaction can be used.
- the solvents are halogenated lower alkanes such as methylene chloride, chloroform, carbon tetrachloride and the like; aromatic hydrocarbons such as benzene, toluene, xylene and the like. If necessary, basic compounds such as trialkylamine, pyridine and the like may be used as suitable condensation agent.
- the ratio of amount of the allophanoyl chloride and the amine in this reaction is not subjected to any specific restriction and may be suitably selected from a wide range, and usually it is desirable that the amine (7) or (9) is used in equimolar to 2 times the molar quantity of the allophanoyl chloride (6) or (8).
- the reaction temperature is also not subjected to any particular restriction, and the reaction can advantageously be carried out at -20° to +50° C.
- 1,3,5-substituted biuret compound of the formula (1) can be isolated by usual separation means.
- the allophanoyl chloride of the formula (6) or (8) used as the starting material in the reaction process--B is usually known compound and if necessary, it can be prepared by reacting the urea compound of the formula (2) or (4) used in the reaction process--A with phosgene according to known method [e.g. J. Org. Chem., vol. 29, pp. 2401 (1964)].
- the reaction of the 1,3-diazetidine-2,4-dione with the amine may usually be carried out in a solvent.
- the solvent used in this reaction is not subjected to any specific restriction and any known inert type which gives no adverse effect to the reaction can be used. Generally, water, acetone, acetonitrile and the like may be used as the solvent.
- the ratio of amount of the 1,3-diazetidine-2,4-dione and the amine in this reaction is not subjected to any specific restriction and may be suitably selected from a wide range, and usually, it is desirable that the amine (7) or (9) is used in equimolar to 2 times the molar quantity of the 1,3-diazetidine-2,4-dione (10) or (11).
- the reaction temperature is also not subjected to any particular restriction, and the reaction can advantageously be carried out at a room temperature to about 100° C.
- the thus formed 1,3,5-substituted biuret compound of the formula (1) can be isolated by usual separation means.
- the 1,3-diazetidine-2,4-dione of the formula (10) or (11) used as the starting material in the reaction process--C is usually known compound and if necessary, it can be prepared by reacting the allophanoyl chloride compound of the formula (6) or (8) in the reaction process--B with boron trichloride according to known method [e.g. Angew. Chem. International Edition, vol. 9, pp. 373 (1970)].
- the reaction of the 1,3,5-oxadiazine-2,4,6-trione with the amine may usually be carried out in a solvent.
- the solvent used in this reaction is not subjected to any specific restriction and any known inert type which gives no adverse effect to the reaction can be used.
- acetonitrile, tetrahydrofuran and the like may be used as the solvent.
- the ratio of amount of the 1,3,5-oxadiazine-2,4,6-trione and the amine in this reaction is not subjected to any specific restriction and may be suitably selected from a wide range, and usually, it is desirable that the amine (7) or (9) is used in equimolar to 2 times the molar quantity of the 1,3,5-oxadiazine-2,4,6-trione (12) or (13).
- the reaction temperature is also not subjected to any particular restriction, and the reaction can advantageously be carried out at a room temperature to about 100° C.
- the thus formed 1,3,5-oxadiazine-2,4,6-trione of the formula (1) can be isolated by usual separation means.
- the 1,3,5-oxadiazine-2,4,6-trione of the formula (12) or (13) used as the starting material in this reaction process--D is usually known compound and if necessary, it can easily be prepared by reacting the isocyanate of the formula (3) or (5) used in the reaction process--A with carbon dioxide according to known method [e.g. Bull. Soc. Chim. Fr., 1974, 1497].
- 1,3,5-substituted biuret compounds of the formula (1) of the present invention are useful as analgesic agents, anti-inflammatory agents or anti-pyretic agents.
- 1,3,5-substituted biuret compounds of the formula (1') ##STR8## wherein R 1 .spsp.' is a lower alkyl group, a substituted lower alkyl group having chlorine atoms(s), cyano group(s), dimethylamino group(s) or hydroxyl group(s) as the substituent(s), a lower alkenyl group or a methoxy group;
- R 2 is a hydrogen atom, a lower alkyl group, or a phenyl group;
- R 3 .spsp.' is a phenyl group, a substituted phenyl group having halogen atom(s), trifluoromethyl group(s), methoxy group(s),
- the 1,3,5-substituted biuret compound of the formula (1) of the present invention can be administered in the range of from 10 to 2,000 mg per day, preferably from 50 to 1,000 mg per day, for an adult, as a analgesic, anti-inflamatory or anti-pyretic agent.
- the administration of the compound is carried out by dividing the above-mentioned daily dosage into 2 or 3 portions. Said dosage of the compound may be adjusted in consideration of the clinical conditions and age of the patient.
- the administration may be carried out in the form of peroral preparations, injection preparations, suppository preparations for rectal use, topical preparations and the like.
- An analgesic, anti-inflammatory or anti-pyretic composition containing the present 1,3,5-substituted biuret compound of the formula (1) is prepared and administered by formulating with conventional pharmaceutically acceptable carriers or excipients through a common method.
- Peroral preparations such as tablets, capsules, granules, powders, etc. may contain excipients used generally in the art. Said excipients are exemplified such as calcium carbonate, calcium phasphates, starch, sucrose, lactose, talc, magnesium stearate, gelatine, polyvinylpyrrolidone, gum arabic, sarbitol, microcrystalline cellulose, polyethyleneglycol, carboxymethylcellulose, silica polyvinylacetal diethylamino acetate, hydroxypropyl methylcellulose, shellac, etc. Further, the tablets may be coated with a suitable coating by a common method known in the arts.
- Peroral liquid form preparations may be of aqueous or oily suspensions, syrups, elixiers and the like and are prepared by common methods.
- Injection preparations may be of aqueous or oily suspensions, powdery or lyophilyzed preparations which is dissolved upon use. These preparations may be prepared by a common method.
- the present substituted biuret compound may be administered as a suppository composition for rectal use, which may be contain pharmaceutically acceptable carriers, known in the art, such as polyethylene glycols, lanoline, cacao butter, fatty acid triglycerides, and the like.
- pharmaceutically acceptable carriers known in the art, such as polyethylene glycols, lanoline, cacao butter, fatty acid triglycerides, and the like.
- the substituted biuret compound of the formula (1) of the present invention may be administered in the form of an ointment or cream which is prepared by formulating with a suitable ointment base and other additives by common method.
- the present invention is further explained in detail by illustrating examples of synthesis of the substituted biuret compounds in Table 1; and pharmacological tests including analgesic activity test, anti-inflammatory activity test and anti-pyretic activity test in Table 2 together with examples of pharmaceutical preparations.
- mice The ddy strain of male mice (body weight, 20-25 g) were used as test animals. The mice were fasted overnight and the compound to be tested was administered orally. General symptom of the mouse after the administration was observed for 7 days.
- the lethal dose (mg/kg, body weight) of the test compound was determined in connection with the death number of mice/the number of mice tested. In Table 2, the values indicated with ⁇ marks are 50% lethal dose, LD 50 (mg/kg, body weight).
- Anti-pyretic activity of the test compound was determined as the FI (febril index) by integrating pyrogenetic curve up to 4 hours after the administration of the test compound with time, and indicated as inhibitory ratio (%) shown by the following formula, ##EQU1##
- mice were used as test animals.
- the mice were fasted overnight, 100 mg/kg body weight of the test compound was administered orally, then 1 hour after the administration, 0.2 ml of 0.7% acetic acid solution was injected intraperitoneally. The acetic acid-induced stretching symptom of mouse was observed.
- Analgesic activity of the test compound was calculated as the inhibitory ratio (%).
- Table 2 the values in parentheses show the data obtained from the test by using the dosage other than 100 mg/kg body weight. Further, the values indicated with ⁇ marks show 50% effective dose, ED 50 (mg/kg body weight).
- the ddy strain of male mice (body weight, 20-25 g) were used as test animals.
- the mice were fasted overnight, 100 mg/kg body weight of the test compound was administered orally, then 45 minutes after the administration, the threshhold amount (1.5-2.5 mg/kg body weight) of morphine hydrochloride was injected subcutaneously. Then 1-hour pain reaction of the mouse caused by a clamp was observed.
- Analgesic activity of the test compound was calculated as the inhibitory ratio (%).
- Table 2 the values in parentheses show the data obtained from the test by using the dosage other than 100 mg/kg body weight. Further, the values indicated with ⁇ marks show 50% effective dose, ED 50 (mg/kg body weight).
- the Wistar strain of male rats (body weight, 150-180 g) were used as test animals.
- the rats were fasted overnight, 100 mg/kg body weight of the test compound was administered orally, then 1 hour after the administration, 0.1 ml of 1% carrageenin solution, as the inflammation inducing agent, was injected subcutaneously to the hindpaw of the rat and the volume of the hindpaw was measured at time sequences.
- Anti-inflammatory activity of the test compound was calculated as inflammation inhibitory ratio (%) at 3 hours after the injection of inflammation inducing agent.
- compositions containing 1,3,5-substituted biuret compound of the formula (1) as the active ingredient.
- granular preparation is prepared by conventional methods.
- tablet preparation is prepared by conventional methods.
- a capsule preparation is prepared by conventional methods.
- a capsule preparation is prepared by conventional methods.
- a suppository preparation is prepared by conventional methods.
- an injection preparation (ampule) is prepared by conventional methods.
- an ointment preparation is prepared by conventional methods.
- tablet preparation is prepared by conventional methods.
- a capsule preparation is prepared by conventional methods.
- a capsule preparation is prepared by conventional method.
- a suppository preparation is prepared by conventional methods.
- an injection preparation (ampule) is prepared by conventional methods.
- an ointment preparation is prepared by conventional methods.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
An analgesic, anti-inflammatory or anti-pyretic composition containing 1,3,5-substituted biuret compound of the formula, <IMAGE> wherein R1 is a hydrogen atom, a lower alkyl group, a substituted lower alkyl group having chlorine atom(s), cyano group(s), dimethylamino group(s), hydroxy group(s), methoxy group(s) or carboxy group(s) as the substituent(s), a lower alkenyl group, a hydroxy group, a methoxy group, an acetyl group or a phenyl group; R2 is a hydrogen atom, a lower alkyl group or a phenyl group; R3 is a phenyl group, a substituted phenyl group having halogen atom(s), trifluoromethyl group(s), methyl group(s), methoxy group(s), methylenedioxy group(s), hydroxy group(s), dimethylamino group(s), carboxy group(s) or carboxymethyl group(s) as the substituent(s), a benzyl group, a pyridyl group, a substituted pyridyl group having methyl group(s) as the substituent(s), a pyridylmethyl group, pyrimidinyl group, a thiazolyl group or a thienyl group, as the active ingredient.
Description
This is a Divisional application of Ser. No. 134,411, filed Mar. 27, 1980.
The present invention relates to a pharmaceutical composition containing a 1,3,5-substituted biuret compound. More particularly, the present invention relates to an analgesic, anti-inflammatory or anti-pyretic composition containing as the active ingredient 1,3,5-substituted biuret compound of the formula (1), ##STR2## wherein R1 is a hydrogen atom, a lower alkyl group, a substituted lower alkyl group having chlorine atom(s), cyano group(s), dimethylamino group(s), hydroxy group(s), methoxy group(s) or carboxy group(s) as the substituent(s), a lower alkenyl group, a hydroxy group, a methoxy group, an acetyl group or a phenyl group; R2 is a hydrogen atom, a lower alkyl group or a phenyl group; R3 is a phenyl group, a substituted phenyl group having halogen atom(s), trifluoromethyl group(s), methyl group(s), methoxy group(s), methlenedioxy group(s), hydroxy group(s), dimethylamino group(s), carboxyl group(s) or carboxymethyl group(s) as the substituent(s), a benzyl group, a pyridyl group, a substituted pyridyl group having methyl group(s) as the substituent(s), a pyridylmethyl group, a pyrimidinyl group, a thiazolyl group or a thienyl group.
Hitherto, some of 1,3,5-substituted biuret compounds represented by the formula (1) are known. On the other hand, although the definitions of the substituents in the formula (1) are different, other substituted biuret compounds having the basic structure of the formula, ##STR3## which is common to the formula (1) are known.
There have been reported that some of such known substituted biuret compounds, especially the latter compounds having the above-mentioned basic structure, have hypotensive, sedative or anti-convulsive activity. However, the prior art has not been aware that either 1,3,5-substituted biuret compounds represented by the general formula (1) or other known biuret compounds, having the above-mentioned basic structure which is common to the general formula (1), have analgesic, anti-inflammatory or anti-pyretic activity. [cf. British pat. No. 1,096,006; British Pat. No. 819,853 and J. Amer. Chem. Soc., 62, 1595 (1940)]
The present invention is based on the facts that the 1,3,5-substituted biuret compounds represented by the general formula have analgesic, anti-inflammatory or anti-pyretic activity.
The object of the present invention is to provide novel 1,3,5-substituted biuret compounds.
Another object of the present invention is to provide an analgesic, anti-inflammatory or anti-pyretic composition containing 1,3,5-substituted biuret compound as the active ingredient.
Among the 1,3,5-substituted biuret compounds of the formula (1), the following compounds are novel ones.
1,3-Dimethyl-5-(2-chlorophenyl)biuret
1,3-Dimethyl-5-(2-trifluoromethylphenyl)biuret
1,3-Dimethyl-5-(3,4-methylenedioxyphenyl)biuret
1,3-Dimethyl-5-(2-carboxyphenyl)biuret
1,3-Dimethyl-5-(4-carboxymethylphenyl)biuret
1,3-Dimethyl-5-(2-pyridylmethyl)biuret
1,3-Dimethyl-5-(4-methyl-2-pyridyl)biuret
1,3-Dimethyl-5-(2-pyrimidinyl)biuret
1-Methyl-3-ethyl-5-phenylbiuret
1-Ethyl-5-phenylbiuret
1-Ethyl-5-(2-chlorophenyl)biuret
1-Ethyl-5-(3-chlorophenyl)biuret
1-Ethyl-5-(3,4-dichlorophenyl)biuret
1-Ethyl-5-(4-methoxyphenyl)biuret
1-Ethyl-5-benzylbiuret
1-Ethyl-5-(2-pyridyl)biuret
1-Ethyl-3-methyl-5-phenylbiuret
1-Ethyl-3-methyl-5-(4-fluorophenyl)biuret
1-Ethyl-3-methyl-5-(4-dimethylaminophenyl)biuret
1-Ethyl-3-methyl-5-(4-hydroxyphenyl)biuret
1-Ethyl-3-methyl-5-(4-methoxyphenyl)biuret
1-Ethyl-3-methyl-5-(3,4-dimethoxyphenyl)biuret
1-Ethyl-3-methyl-5-(3,4,5-trimethoxyphenyl)biuret
1-Ethyl-3-methyl-5-(4-methylphenyl)biuret
1-Ethyl-3-methyl-5-(3,4-dimethylphenyl)biuret
1-Ethyl-3-methyl-5-(2-thenyl)biuret
1-n-Propyl-3-methyl-5-phenylbiuret
1-Isopropyl-3-methyl-5-phenylbiuret
1-Propenyl-5-phenylbiuret
1-Propenyl-3-methyl-5-phenylbiuret
1-n-Propyl-5-phenylbiuret
1-n-Propyl-3-methyl-5-phenylbiuret
1-n-Propyl-5-benzylbiuret
1-Isobutyl-3-methyl-5-phenylbiuret
1-(1-Methylpropyl)-3-methyl-5-phenylbiuret
1-tert-Butyl-3-methyl-5-phenylbiuret
1-n-Pentyl-3-methyl-5-phenylbiuret
1-(2-Chloroethyl)-3-methyl-5-phenylbiuret
1-(2-Cyanoethyl)-3-methyl-5-phenylbiuret
1-(2-Dimethylaminoethyl)-3-methyl-5-phenylbiuret
1-(2-Hydroxyethyl)-3-methyl-5-phenylbiuret
1-(2-Methyl-2-hydroxypropyl)-3-methyl-5-phenylbiuret
1-(2,3-Dihydroxypropyl)-3-methyl-5-phenylbiuret
1-(2-Methoxyethyl)-3-methyl-5-phenylbiuret
1-Carboxymethyl-3-methyl-5-phenylbiuret
1-Acetyl-3-methyl-5-phenylbiuret
1-Hydroxy-3-methyl-5-phenylbiuret
1-Methoxy-3-methyl-5-phenylbiuret
The 1,3,5-substituted biuret compound of the formula (1) can be prepared by any processes shown below.
Reaction of an urea compound of the formula (2) or (4) with an isocyanate of the formula (3) or (5) to obtain the 1,3,5-substituted biuret compound of the formula (1) is shown as follows: ##STR4##
In this reaction process A, the reaction of the urea with the isocyanate may be carried out in the presence or absence of a solvent. The solvent used in this reaction is not subjected to any specific restriction and any known inert type which gives no adverse effect to the reaction can be used. Among the examples of the solvents are ethers such as ether, dioxane, tetrahydrofuran and the like; halogenated lower alkanes such as methylene chloride, chloroform, carbon tetrachloride and the like; aromatic hydrocarbons such as benzene, toluene, xylene and the like. The ratio of amount of the urea and the isocyanate in this reaction is not subjected to any specific restriction and may be suitably selected from a wide range, and usually, it is desirable that they are used in equimolar quantity respectively. The reaction temperature is also not subjected to any particular restriction and may be suitably selected from a wide range, and usually the reaction can advantageously be carried out at a room temperature to the boiling point of the solvent used generally within the range of 20° to 200° C. The obtained 1,3,5-substituted biuret compound of the formula (1) can be isolated by usual separation means.
Reaction of an allophanoyl chloride of the formula (6) or (8) with an amine of the formula (7) or (9) to obtain 1,3,5-substituted biuret compound of the formula (1) is shown as follows: ##STR5##
In this reaction process B, the reaction of the allophanoyl chloride with the amine may be carried out in a solvent. The solvent used in this reaction is not subjected to any specific restriction and any known inert type which gives no adverse effect to the reaction can be used. Among the examples of the solvents are halogenated lower alkanes such as methylene chloride, chloroform, carbon tetrachloride and the like; aromatic hydrocarbons such as benzene, toluene, xylene and the like. If necessary, basic compounds such as trialkylamine, pyridine and the like may be used as suitable condensation agent. The ratio of amount of the allophanoyl chloride and the amine in this reaction is not subjected to any specific restriction and may be suitably selected from a wide range, and usually it is desirable that the amine (7) or (9) is used in equimolar to 2 times the molar quantity of the allophanoyl chloride (6) or (8). The reaction temperature is also not subjected to any particular restriction, and the reaction can advantageously be carried out at -20° to +50° C. Thus formed 1,3,5-substituted biuret compound of the formula (1) can be isolated by usual separation means.
The allophanoyl chloride of the formula (6) or (8) used as the starting material in the reaction process--B is usually known compound and if necessary, it can be prepared by reacting the urea compound of the formula (2) or (4) used in the reaction process--A with phosgene according to known method [e.g. J. Org. Chem., vol. 29, pp. 2401 (1964)].
Reaction of a 1,3-diazetidine-2,4-dione of the formula (10) or (11) with an amine of the formula (7) or (9) to obtain 1,3,5-substituted biuret compound of the formula (1) is shown as follows: ##STR6##
In this reaction process--C, the reaction of the 1,3-diazetidine-2,4-dione with the amine may usually be carried out in a solvent. The solvent used in this reaction is not subjected to any specific restriction and any known inert type which gives no adverse effect to the reaction can be used. Generally, water, acetone, acetonitrile and the like may be used as the solvent. The ratio of amount of the 1,3-diazetidine-2,4-dione and the amine in this reaction is not subjected to any specific restriction and may be suitably selected from a wide range, and usually, it is desirable that the amine (7) or (9) is used in equimolar to 2 times the molar quantity of the 1,3-diazetidine-2,4-dione (10) or (11). The reaction temperature is also not subjected to any particular restriction, and the reaction can advantageously be carried out at a room temperature to about 100° C. The thus formed 1,3,5-substituted biuret compound of the formula (1) can be isolated by usual separation means. The 1,3-diazetidine-2,4-dione of the formula (10) or (11) used as the starting material in the reaction process--C is usually known compound and if necessary, it can be prepared by reacting the allophanoyl chloride compound of the formula (6) or (8) in the reaction process--B with boron trichloride according to known method [e.g. Angew. Chem. International Edition, vol. 9, pp. 373 (1970)].
When preparing 1,3,5-substituted biuret compound of the formula (1), wherein R1 =R2 or R2 =R3, it is prepared by reacting a 1,3,5-oxadiazine-2,4,6-trione of the formula (12) or (13) with an amine of the formula (7) or (9) as follows: ##STR7##
In this reaction process--D, the reaction of the 1,3,5-oxadiazine-2,4,6-trione with the amine may usually be carried out in a solvent. The solvent used in this reaction is not subjected to any specific restriction and any known inert type which gives no adverse effect to the reaction can be used. Generally, acetonitrile, tetrahydrofuran and the like may be used as the solvent. The ratio of amount of the 1,3,5-oxadiazine-2,4,6-trione and the amine in this reaction is not subjected to any specific restriction and may be suitably selected from a wide range, and usually, it is desirable that the amine (7) or (9) is used in equimolar to 2 times the molar quantity of the 1,3,5-oxadiazine-2,4,6-trione (12) or (13). The reaction temperature is also not subjected to any particular restriction, and the reaction can advantageously be carried out at a room temperature to about 100° C. The thus formed 1,3,5-oxadiazine-2,4,6-trione of the formula (1) can be isolated by usual separation means.
The 1,3,5-oxadiazine-2,4,6-trione of the formula (12) or (13) used as the starting material in this reaction process--D is usually known compound and if necessary, it can easily be prepared by reacting the isocyanate of the formula (3) or (5) used in the reaction process--A with carbon dioxide according to known method [e.g. Bull. Soc. Chim. Fr., 1974, 1497].
Most of the 1,3,5-substituted biuret compounds of the formula (1) of the present invention [that is, all compounds, except those of formula (1') below] are useful as analgesic agents, anti-inflammatory agents or anti-pyretic agents. However, among of those compounds, 1,3,5-substituted biuret compounds of the formula (1') ##STR8## wherein R1.spsp.' is a lower alkyl group, a substituted lower alkyl group having chlorine atoms(s), cyano group(s), dimethylamino group(s) or hydroxyl group(s) as the substituent(s), a lower alkenyl group or a methoxy group; R2 is a hydrogen atom, a lower alkyl group, or a phenyl group; R3.spsp.' is a phenyl group, a substituted phenyl group having halogen atom(s), trifluoromethyl group(s), methoxy group(s), methylenedioxy group(s), dimethylamino group(s) or hydroxy group(s) as the substituent(s), a benzyl group, a pyridyl group, a substituted pyridyl group having methyl group(s) as the substituent(s), a thiazolyl group or a thienyl group, are useful only as anti-inflammatory agents.
The 1,3,5-substituted biuret compound of the formula (1) of the present invention can be administered in the range of from 10 to 2,000 mg per day, preferably from 50 to 1,000 mg per day, for an adult, as a analgesic, anti-inflamatory or anti-pyretic agent. The administration of the compound is carried out by dividing the above-mentioned daily dosage into 2 or 3 portions. Said dosage of the compound may be adjusted in consideration of the clinical conditions and age of the patient.
The administration may be carried out in the form of peroral preparations, injection preparations, suppository preparations for rectal use, topical preparations and the like.
An analgesic, anti-inflammatory or anti-pyretic composition containing the present 1,3,5-substituted biuret compound of the formula (1) is prepared and administered by formulating with conventional pharmaceutically acceptable carriers or excipients through a common method.
Peroral preparations such as tablets, capsules, granules, powders, etc. may contain excipients used generally in the art. Said excipients are exemplified such as calcium carbonate, calcium phasphates, starch, sucrose, lactose, talc, magnesium stearate, gelatine, polyvinylpyrrolidone, gum arabic, sarbitol, microcrystalline cellulose, polyethyleneglycol, carboxymethylcellulose, silica polyvinylacetal diethylamino acetate, hydroxypropyl methylcellulose, shellac, etc. Further, the tablets may be coated with a suitable coating by a common method known in the arts. Peroral liquid form preparations may be of aqueous or oily suspensions, syrups, elixiers and the like and are prepared by common methods. Injection preparations may be of aqueous or oily suspensions, powdery or lyophilyzed preparations which is dissolved upon use. These preparations may be prepared by a common method.
The present substituted biuret compound may be administered as a suppository composition for rectal use, which may be contain pharmaceutically acceptable carriers, known in the art, such as polyethylene glycols, lanoline, cacao butter, fatty acid triglycerides, and the like.
As to preparations for topical use, the substituted biuret compound of the formula (1) of the present invention may be administered in the form of an ointment or cream which is prepared by formulating with a suitable ointment base and other additives by common method.
The present invention is further explained in detail by illustrating examples of synthesis of the substituted biuret compounds in Table 1; and pharmacological tests including analgesic activity test, anti-inflammatory activity test and anti-pyretic activity test in Table 2 together with examples of pharmaceutical preparations.
In 50 ml of anhydrous dioxane, 3.5 g (0.04 mol) of ethyl urea was dissolved, and under stirring 4.8 g (0.04 mol) of phenylisocyanate was added thereinto. The reaction was carried out at a room temperature for 15 hours, then the solvent was removed by distillation under a reduced pressure. The residue thus obtained was recrystallized from ethanol-water to obtain 4.6 g (yield 55%) of 1-ethyl-5-phenylbiuret having a melting point of 80°-81.5° C.
In 50 ml of anhydrous dioxane, 3.5 g (0.04 mol) of 1,3-dimethyl urea was dissolved, and under stirring 4.8 g (0.04 mol) of phenylisocyanate was added thereinto. The reaction was carried out at a room temperature for 15 hours, then the reaction mixture was treated a procedure same as in Example 1. The residue thus obtained was recrystallized from ethanol-petroleum ether to obtain 5.0 g (yield 60%) of 1,3-dimethyl-5-phenylbiuret having a melting point of 93°-95° C.
In 50 ml of anhydrous tetrahydrofuran, 9.0 g (0.2 mol) of ethylamine was dissolved, and under cooling below 0° C. with stirring, a solution prepared by dissolving 21.3 g (0.1 mol) of 2-methyl-4-phenylallophanoyl chloride into 50 ml of anhydrous tetrahydrofuran was added by drop-wise. The reaction was continued at a room temperature for 1 hour, the solvent was then removed by distillation under a reduced pressure. To the residue thus obtained was added water and the precipitate thus formed was separated by filtration and dried, and recrystallized from ether-petroleum ether to obtain 17.7 g (yield 80%) of 1-ethyl-3-methyl-5-phenylbiuret having a melting point of 80.5°-81.5° C.
In 30 ml of acetonitrile, 6.0 g (0.025 mol) of 1,3-diphenyl-1,3-diazetidine-2,4-dione was added. Then 3.9 ml (0.05 mol) of aqueous solution (40%) of methylamine was added dropwise thereinto with stirring. The reaction was continued at 50° C. for 0.5 hours, then the solvent was removed by distillation under a reduced pressure. The residue thus obtained was recrystallized from ethanol to obtain 5.1 l g (yield 76%) of 1-methyl-3,5-diphenylbiuret having a melting point of 145°-147° C.
In 50 ml of acetonitrile, 5.0 g (0.0316 mol) of 3,5-dimethyl-2,4,6-trioxohydro-1,3,5-oxadiazine and 3.0 g (0.0319 mol) of 2-aminopyridine were added. The reaction was continued under refluxing condition for 7 hours. After the reaction was completed, water was added to the reaction mixture and was filtered. The filtrate thus obtained was extracted with chloroform, and the extracted liquid was dried with anhydrous sodium sulfate and the chloroform was removed by distillation. The residue thus obtained was recrystallized from benzene to obtain 3.0 g (yield 46%) of 1,3-dimethyl-5-(2-pyridyl)biuret having a melting point of 112°-115° C.
In the following Table 1, there are mentioned the physico-chemical properties of 1,3,5-substituted biuret compounds of the formula (1) including the compounds prepared in Examples 1-5.
TABLE 1
__________________________________________________________________________
poundCom-
##STR9## pro-tionReac-
Mp,
UVλ .sub.max.sup.Cyclohexane
Molecular
(Found)CalculatedEleme
ntal analysis (%)
No.
R.sup.1 R.sup.2
R.sup.3 cess
(°C.)
mμ (ε)
formula C H N
__________________________________________________________________________
1*
H CH.sub.3
##STR10##
B 188- 190
243.5 (17700)
C.sub.9 H.sub.11 N.sub.3
55.95 (55.62)
5.74 (5.57)
21.75 (21.61)
2*
CH.sub.3 H
##STR11##
A 121- 122
240 (19600)
C.sub.9 H.sub.11 N.sub.3
55.95 (55.91)
5.74 (5.59)
21.75 (21.77)
3*
CH.sub.3 CH.sub.3
##STR12##
A 93-95
244 (17900)
C.sub.10 H.sub.13 N.sub.3
O.sub.2 57.96 (58.09)
6.32 (6.39)
20.28 (20.18)
4*
CH.sub.3 CH.sub.3
##STR13##
B 148- 150
240.5 (25800)
C.sub.10 H.sub.12 FN.sub.3
O.sub.2 53.33 (53.22)
5.37 (5.30)
18.66 (18.32)
5
CH.sub.3 CH.sub.3
##STR14##
A 168.5- 170.5
247.5 (20700)
C.sub.10 H.sub.12 ClN.sub.3
O.sub.2 49.70 (49.99)
5.00 (4.96)
17.39 (17.32)
6*
CH.sub.3 CH.sub.3
##STR15##
A 143- 145
250.5 (25000)
C.sub.10 H.sub.12 ClN.sub.3
O.sub.2 49.70 (49.70)
5.00 (5.09)
17.39 (17.18)
7
CH.sub.3 CH.sub.3
##STR16##
B 115- 117
243 (17200)
C.sub.11 H.sub.12 F.sub.3
N.sub.3 O.sub.2
48.00 (48.30)
4.39 (4.43)
15.27 (15.38)
8*
CH.sub.3 CH.sub.3
##STR17##
B 110- 111
249 (20300)
C.sub.11 H.sub.15 N.sub.3
O.sub.3 55.69 (55.66)
6.37 (6.63)
17.71 (17.50)
9
CH.sub.3 CH.sub.3
##STR18##
B 176- 178
256 (13500)
C.sub.11 H.sub.13 N.sub.3
O.sub.4 52.59 (52.61)
5.22 (5.19)
16.72 (16.43)
10
CH.sub.3 CH.sub.3
##STR19##
B 178- 179
250 (16400)
C.sub.11 H.sub.13 N.sub.3
O.sub.4 52.59 (52.58)
5.22 (5.12)
16.72 (16.70)
11
CH.sub.3 CH.sub.3
##STR20##
D 195- 196
248.5 (21600)
C.sub.12 H.sub.15 N.sub.3
O.sub.4 54.33 (54.29)
5.70 (5.95)
15.84 (15.79)
12*
CH.sub.3 CH.sub.3
##STR21##
B 118- 119 C.sub.11 H.sub.15 N.sub.3
O.sub.2 59.71 (59.70)
6.83 (7.01)
18.99 (18.97)
13
CH.sub.3 CH.sub.3
##STR22##
D 101.5- 102.5
262 (2700)
C.sub.10 H.sub.14 N.sub.4
O.sub.2 54.04 (54.14)
6.35 (6.26)
25.21 (25.41)
14*
CH.sub.3 CH.sub.3
##STR23##
D 112- 115
238 (19400)
C.sub.9 H.sub.12 N.sub.4
51.92 (51.88)
5.81 (5.93)
26.91 (27.04)
15*
CH.sub.3 CH.sub. 3
##STR24##
D 149- 150
242 (15400)
C.sub.9 H.sub.12 N.sub.4
51.92 (52.01)
5.81 (5.74)
26.91 (26.95)
16*
CH.sub.3 CH.sub.3
##STR25##
D 177- 178 C.sub.9 H.sub.12 N.sub.4
51.92 (51.80)
5.81 (5.88)
26.91 (27.00)
17*
CH.sub.3 CH.sub.3
##STR26##
D 146- 147
239 (19200)
C.sub.10 H.sub.14 N.sub.4
O.sub.2 54.04 (53.86)
6.35 (6.38)
25.21 (25.20)
18
CH.sub.3 CH.sub.3
##STR27##
D 120- 121.5
240 (20300)
C.sub.10 H.sub.14 N.sub.4
O.sub.2 54.04 (53.73)
6.35 (6.42)
25.21 (25.16)
19
CH.sub.3 CH.sub.3
##STR28##
D 229- 231 (de- com- posed)
272 (3100)
C.sub.8 H.sub.11 N.sub.5
O.sub.2.HCl
39.13 (38.92)
4.93 (5.03)
28.52 (28.67)
20*
CH.sub.3 CH.sub.3
##STR29##
D 166- 167
263 (11500)
C.sub.7 H.sub.10 N.sub.4 O.sub.2
S 39.24 (39.26)
4.70 (4.81)
26.15 (26.03)
21
CH.sub.3 C.sub.2 H.sub.5
##STR30##
B 84-86
244 (19700)
C.sub.11 H.sub.15 N.sub.3
O.sub.2 59.71 (60.06)
6.83 (7.05)
18.99 (19.13)
22*
CH.sub.3
##STR31##
##STR32##
C 145- 147 C.sub.15 H.sub.15 N.sub.3
O.sub.2 66.90 (66.70)
5.61 (5.54)
15.60 (15.53)
23
C.sub.2 H.sub.5
H
##STR33##
A 80-81.5
242 (21700)
C.sub.10 H.sub.13 N.sub.3
O.sub.2 57.96 (58.05)
6.32 (6.48)
20.28 (20.25)
24
C.sub.2 H.sub.5
H
##STR34##
A 152- 154
245.5 (20300)
C.sub.10 H.sub.12 ClN.sub.3
O.sub.2 49.70 (49.95)
5.00 (4.86)
17.39 (17.08)
25
C.sub.2 H.sub.5
H
##STR35##
A 120- 122
244.5 (22300)
C.sub.10 H.sub.12 ClN.sub.3
O.sub.2 49.70 (49.98)
5.00 (4.82)
17.39 (17.25)
26*
C.sub.2 H.sub.5
H
##STR36##
A 175- 177
248 (25900)
C.sub.10 H.sub.12 ClN.sub.3
O.sub.2 49.70 (49.97)
5.00 (5.13)
17.39 (17.24)
27
C.sub.2 H.sub.5
H
##STR37##
A 184.5- 185.5
250.5 (26600)
C.sub.10 H.sub.11 Cl.sub.2
N.sub.3 O.sub.2
43.50 (43.30)
4.02 (4.01)
15.22 (15.22)
28
C.sub.2 H.sub.5
H
##STR38##
A 141- 142
248 (21400)
C.sub.11 H.sub.17 N.sub.3
O.sub.4 55.69 (55.60)
6.37 (6.13)
17.71 (17.41)
29
C.sub.2 H.sub.5
H
##STR39##
A 108- 110 C.sub.11 H.sub.15 N.sub.3
O.sub.2 59.71 (59.85)
6.83 (6.89)
18.88 (19.14)
30
C.sub.2 H.sub.5
H
##STR40##
A 125- 126
240 (19800)
C.sub.9 H.sub.12 N.sub.4
51.92 (51.83)
5.81 (5.94)
26.91 (26.80)
31
C.sub.2 H.sub.5
CH.sub.3
##STR41##
B 80.5- 81.5
244 (19900)
C.sub.11 H.sub.15 N.sub.3
O.sub.2 59.71 (59.78)
6.83 (7.03)
18.99 (18.69)
32
C.sub.2 H.sub.5
CH.sub.3
##STR42##
B 112- 114
241 (20000)
C.sub.11 H.sub.14 FN.sub.3
O.sub.2 55.22 (55.08)
5.90 (6.04)
17.56 (17.24)
33
C.sub.2 H.sub.5
CH.sub.3
##STR43##
B 116- 118
263 (22300)
C.sub.13 H.sub.20 N.sub.4
O.sub.2 59.07 (58.93)
7.63 (7.61)
21.20 (21.20)
34
C.sub.2 H.sub.5
CH.sub.3
##STR44##
B 151- 153
248 (15100)
C.sub.11 H.sub.15 N.sub.3
O.sub.3 55.69 (55.60)
6.37 (6.29)
17.71 (17.80)
35
C.sub.2 H.sub.5
CH.sub.3
##STR45##
B 58- 59
249 (22000)
C.sub.12 H.sub.17 N.sub.3
O.sub.3 57.36 (57.13)
6.82 (6.96)
16.72 (16.41)
36
C.sub.2 H.sub.5
CH.sub.3
##STR46##
B 98-100
252 (14700)
C.sub.13 H.sub.19 N.sub.3
O.sub.4 55.51 (55.63)
6.81 (6.87)
14.94 (14.54)
37
C.sub.2 H.sub.5
CH.sub.3
##STR47##
B 104- 106
256 (15400)
C.sub.14 H.sub.19 N.sub.3
O.sub.5 54.01 (53.94)
6.80 (6.79)
13.50 (13.74)
38
C.sub.2 H.sub.5
CH.sub.3
##STR48##
B 88-90
246 (20100)
C.sub.12 H.sub.17 N.sub.3
O.sub.2 61.26 (61.23)
7.28 (7.46)
17.86 (17.61)
39
C.sub.2 H.sub.5
CH.sub.3
##STR49##
B 66-68
247 (18800)
C.sub.13 H.sub.19 N.sub.3
O.sub.2.1/2H.sub.2 O
60.45 (60.07)
7.80 (7.71)
16.27 (16.09)
40
C.sub.2 H.sub.5
CH.sub.3
##STR50##
B 112- 114
271 (11400) 267 (11600)
C.sub.9 H.sub.13 N.sub.3 O.sub.2
S 47.56 (47.78)
5.77 (5.77)
18.49 (18.38)
41
(CH.sub.2).sub.2 CH.sub.3
CH.sub.3
##STR51##
B 74-76
244 (20800)
C.sub.12 H.sub.17 N.sub.3
O.sub.2 61.26 (61.22)
7.28 (7.52)
17.86 (17.47)
42*
(CH.sub.2).sub.2 CH.sub.3
H
##STR52##
A 85.5- 88
not available
C.sub.12 H.sub.17 N.sub.3
O.sub.2 61.26 (61.33)
7.28 (7.20)
17.86 (17.68)
43
CH(CH.sub.3).sub.2
CH.sub.3
##STR53##
B 92- 93.5
243 (20500)
C.sub.12 H.sub.17 N.sub.3
O.sub.2 61.26 (61.67)
7.28 (7.49)
17.86 (17.83)
44
CH.sub.2 CHCH.sub.2
H
##STR54##
A 75-78
253 (20500)
C.sub.11 H.sub.13 N.sub.3
O.sub.2 60.26 (59.95)
5.98 (6.06)
19.17 (19.10)
45
CH.sub.2 CHCH.sub.2
CH.sub.3
##STR55##
B 79-80
243 (19900)
C.sub.12 H.sub.15 N.sub.3
O.sub.2 61.79 (61.75)
6.48 (6.71)
18.01 (18.15)
46
(CH.sub.2).sub.3 CH.sub.3
H
##STR56##
A 106.5- 108.5
241.5 (22400)
C.sub.12 H.sub.17 N.sub.3
O.sub.2 61.26 (61.03)
7.28 (7.19)
17.86 (17.92)
47
(CH.sub.2).sub.3 CH.sub.3
CH.sub.3
##STR57##
B Oily pro- duct
C.sub.13 H.sub.19 N.sub.3
O.sub.2 (a)
48
(CH.sub.2).sub.3 CH.sub.3
H
##STR58##
A 95-96.5 C.sub.13 H.sub.19 N.sub.3
O.sub.2 62.63 (62.66)
7.68 (7.77)
16.85 (16.55)
49
CH.sub.2 CH(CH.sub.3).sub.2
CH.sub.3
##STR59##
B 56.57
243.5 (20800)
C.sub.13 H.sub.19 N.sub.3
O.sub.2 62.63 (62.75)
7.68 (7.96)
16.85 (16.82)
50
##STR60##
CH.sub.3
##STR61##
B 98-100
253 (19900)
C.sub.13 H.sub.19 N.sub.3
O.sub.2 62.63 (62.78)
7.68 (7.96)
16.85 (16.77)
51
C(CH.sub.3).sub.3
CH.sub.3
##STR62##
B 94-95
243 (20100)
C.sub.13 H.sub.19 N.sub.3
O.sub.2 62.63 (62.57)
7.68 (7.84)
16.85 (16.91)
52
(CH.sub.2).sub.4 CH.sub.3
CH.sub.3
##STR63##
B Oily pro- duct
C.sub.14 H.sub.21 N.sub.3
O.sub.2 (b)
53
CH.sub.2 CH.sub.2 Cl
CH.sub.3
##STR64##
B 117- 118
244 (19200)
C.sub.11 H.sub.14 ClN.sub.3
O.sub.2 51.67 (51.66)
5.52 (5.53)
16.43 (16.23)
54
CH.sub.2 CH.sub.2 CN
CH.sub.3
##STR65##
B 116- 118
245 (18800)
C.sub.12 N.sub.14 N.sub.4
O.sub.2 58.53 (58.38)
5.73 (5.59)
22.75 (22.93)
55
CH.sub.2 CH.sub.2 N(CH.sub.3).sub.2
CH.sub.3
##STR66##
B 179 181
245 (19500)
C.sub.13 H.sub.21 ClN.sub.4
O.sub.2 51.91 (51.98)
7.04 (7.14)
18.63 (18.46)
56
CH.sub.2 CH.sub.2 OH
CH.sub.3
##STR67##
B 105- 106
244 (19600)
C.sub.11 H.sub.15 N.sub.3
O.sub.3 55.69 (55.68)
6.37 (6.56)
17.71 (17.85)
57
##STR68##
CH.sub.3
##STR69##
B 117.5- 119
241 (17300)
C.sub.13 H.sub.19 N.sub.3
O.sub.3 58.85 (58.94)
7.22 (7.39)
15.84 (15.66)
58
##STR70##
CH.sub.3
##STR71##
B 96-97
244 (19700)
C.sub.12 H.sub.17 N.sub.3
O.sub.4 53.92 (53.86)
6.41 (6.66)
15.72 (15.65)
59
CH.sub.2 CH.sub.2 OCH.sub.3
CH.sub.3
##STR72##
B 52-53
243 (16600)
C.sub.12 H.sub.17 N.sub.3
O.sub.3 57.36 (57.36)
6.82 (6.84)
16.72 (16.71)
60
CH.sub.2 COOH
CH.sub.3
##STR73##
B 80-82
243 (20900)
C.sub.11 H.sub.13 N.sub.3
O.sub.4.H.sub.2 O
49.07 (48.70)
5.62 (5.63)
15.61 (15.48)
61
##STR74##
CH.sub.3
##STR75##
A 118- 120
274 (12300)
C.sub.11 H.sub.13 N.sub.3
O.sub.3 56.16 (56.19)
5.57 (5.58)
17.86 (18.04)
62
OH CH.sub.3
##STR76##
B 128- 129
245 (18200)
C.sub.9 H.sub.11 N.sub.3
51.67 (51.53)
5.49 (5.30)
20.09 (19.81)
63
OCH.sub.3 CH.sub.3
##STR77##
B 115- 157
243 (17800)
C.sub.10 H.sub.13 N.sub.3
O.sub.3 53.81 (53.76)
5.87 (5.81)
18.82 (18.57)
64*
##STR78##
CH.sub.3
##STR79##
B 106- 106.5 C.sub.15 H.sub.15 N.sub.3
O.sub.2 66.90 (67.06)
5.61 (5.58)
15.60 (15.67)
__________________________________________________________________________
In Table 1, the compounds with * marks are known compounds and thus the remaining compounds are novel ones. Further (a) in the Compound No. 47 and (b) in Compound 52 indicate the following data obtained by NMR and mass-spectrography methods in place of data obtained by elemental analysis.
.sup.(a) NMR(CDCl3)δ: 0.88 (3H, m, N1 --CH2 CH2 CH2 --CH3), 1.00-1.68 (4H, m, N1 --CH2 --CH2 CH2 --CH3), 3.18 (2H, m, N1 --CH2 --CH2 CH2 CH3), 3.18 (3H, s, N3 --CH3), 6.00 (1H, broad, N1 --H), 6.88-7.49 (5H, m, Ar--H), 10.62 (1H, broad s, N5 --N), MS m/e: 249 (M+).
.sup.(b) NMR(CDCl3)δ: 0.88 (3H, broad t, J=6 Hz, N1 --CH2 --CH2 CH2 CH2 --CH3), 1.07-1.92 (6H, m, N1 --CH2 --CH2 CH2 CH2 --CH3), 2.99-3.27 (2H, m, N1 --CH2 --CH2 CH2 CH2 CH3), 3.12 (3H, s, N3 --CH3), 5.89 (1H, broad t, N1 --H), 6.80-7.43 (5H, m, Ar--H), 10.44 (1H, broad s, N5 --H). MS m/e: 263 (M30).
Next, several tests for determining the pharmacological properties, in that acute toxicity, anti-pyretic activity, analgesic activity and anti-inflammatory activity of the present 1,3,5-substituted biuret compounds of the formula (1) were conducted and the test results are shown in Table (2). In the tests, each compounds to be tested was used as a suspension in 0.25% carboxymethylcellulose solution. Methods for testing are explained as follows:
The ddy strain of male mice (body weight, 20-25 g) were used as test animals. The mice were fasted overnight and the compound to be tested was administered orally. General symptom of the mouse after the administration was observed for 7 days. The lethal dose (mg/kg, body weight) of the test compound was determined in connection with the death number of mice/the number of mice tested. In Table 2, the values indicated with Δ marks are 50% lethal dose, LD50 (mg/kg, body weight).
According to the method reported by Tanabe [Folia Pharmacologia Japonica, Vol. 73, pp. 803 (1977)], the Wistar strain of male rats (150-180 g body weight) were used as test animals. The rats were fasted overnight, and 1 ml/100 g (body weight) of 10% dry-yeast suspension were subcutaneously injected on the back of the rats. Five hours afte the injection, the test compound was administered orally, then the body temperature of the rat was measured time sequences. Anti-pyretic activity of the test compound was determined as the FI (febril index) by integrating pyrogenetic curve up to 4 hours after the administration of the test compound with time, and indicated as inhibitory ratio (%) shown by the following formula, ##EQU1##
(1) Acetic acid-induced stretching method
According to the method reported by Koster et.al., [Fed. Proc., Vol. 18, pp. 412 (1959)], the ddy strain of male mice (body weight, 20-25 g) were used as test animals. The mice were fasted overnight, 100 mg/kg body weight of the test compound was administered orally, then 1 hour after the administration, 0.2 ml of 0.7% acetic acid solution was injected intraperitoneally. The acetic acid-induced stretching symptom of mouse was observed. Analgesic activity of the test compound was calculated as the inhibitory ratio (%). In Table 2, the values in parentheses show the data obtained from the test by using the dosage other than 100 mg/kg body weight. Further, the values indicated with Δ marks show 50% effective dose, ED50 (mg/kg body weight).
(2) Haffner method
According to the modified method reported by Fujimura et al., [Bulletin of the Institute for Chemical Research, Kyoto University, No. 25, pp. 36 (1951)], the ddy strain of male mice (body weight, 20-25 g) were used as test animals. The mice were fasted overnight, 100 mg/kg body weight of the test compound was administered orally, then 45 minutes after the administration, the threshhold amount (1.5-2.5 mg/kg body weight) of morphine hydrochloride was injected subcutaneously. Then 1-hour pain reaction of the mouse caused by a clamp was observed. Analgesic activity of the test compound was calculated as the inhibitory ratio (%). In Table 2, the values in parentheses show the data obtained from the test by using the dosage other than 100 mg/kg body weight. Further, the values indicated with Δ marks show 50% effective dose, ED50 (mg/kg body weight).
According to the method of acute carrageenin-induced inflammatory test [Folia Pharmacologia Japonica, Vol. 56, pp. 575 (1960)], the Wistar strain of male rats (body weight, 150-180 g) were used as test animals. The rats were fasted overnight, 100 mg/kg body weight of the test compound was administered orally, then 1 hour after the administration, 0.1 ml of 1% carrageenin solution, as the inflammation inducing agent, was injected subcutaneously to the hindpaw of the rat and the volume of the hindpaw was measured at time sequences. Anti-inflammatory activity of the test compound was calculated as inflammation inhibitory ratio (%) at 3 hours after the injection of inflammation inducing agent.
TABLE 2
__________________________________________________________________________
Analgesic activity (%)
Anti- Anti-
Acute
Acetic acid- pyretic
inflammatory
Compound
toxicity
induced stretch-
Haffner
activity
activity
No. (mg/kg)
ing method
method (%) (%)
__________________________________________________________________________
1* 2000-2/4
37.5
2* 500-0/4
75 50 28
1000-4/4
3* .sup.Δ 1448
.sup.Δ 35(16-77)
.sup.Δ 111(66-188)
145 88
4* 2000-0/4
37.5 25 79 41
5 2000-0/4
37.5 37.5 28 53
(200 mg/kg)
(200 mg/kg) (200 mg/kg)
6* .sup.Δ 1239
.sup.Δ 40(21-76)
50 72 43
7 1000-0/4
62.5 12.5 121 60
2000-3/4 (200 hours
value)
8* .sup.Δ 1445
87.5 50 110 40
9 .sup.Δ 1084
87.5 25 38 46
10 1000-1/4
12.5
2000-4/4
11 2000-0/4
25 37.5 7
12* 500-0/4
100 50 47
1000-4/4
13 1000-0/4
25 37.5
2000-2/4
14* .sup.Δ 656
62.5 .sup.Δ 145(76-276)
54
15* .sup.Δ 1100
.sup.Δ 44(21-94)
62.5 94 37
16* .sup.Δ 1100
62.5 25 34
17* 1000-0/4
25 25 55 33
2000-3/4
18 .sup.Δ 1500
75 25 60 20
19 .sup.Δ 1400
50 37.5 6
20* 1000-3/4
25 25 112 46
21 1000-1/4
50 37.5 56
2000-3/4
22* 2000-0/4
37.5 50 35
(200 mg/kg)
23 2000-0/4
62.5 60 49
(200 mg/kg)
24 2000-0/4
25 37.5 77
(200 mg/kg)
(200 mg/kg) (200 mg/kg)
25 2000-0/4
25 37.5 86
(200 mg/kg)
(200 mg/kg) (200 mg/kg)
26* 2000-0/4
12.5 25 76
(200 mg/kg)
(200 mg/kg) (200 mg/kg)
27 1000-0/4
12.5 12.5 44
2000-1/4
(200 mg/kg)
(200 mg/kg) (200 mg/kg)
28 .sup.Δ 1600
37.5 37.5 75
(200 mg/kg)
(200 mg/kg) (200 mg/kg)
29 1000-0/4
12.5 25 31
2000-1/4
30 1000-0/4 37.5 30
2000-3/4
31 .sup.Δ 1594
.sup.Δ 70(44-112)
.sup.Δ 105(69-159)
149 63
32 1000-2/4
100 37.5 63
2000-4/4
33 1000-0/4
62.5 25 87 30
2000-4/4
34 2000-0/4
25 12.5 19
35 1000-0/4
87.5 62.5 112 19
2000-4/4
36 .sup.Δ 833
50 62.5 43 23
37 .sup.Δ 749
75 .sup.Δ 46(31-69)
97
38 1000-0/4
87.5 25 80
2000-3/4
39 2000-0/4
50 37.5 8
40 .sup.Δ 559
75 37.5 42 24
41 2000-0/4
62.5 37.5 65 67
42* 2000-0/4
82.5 50 31
(200 mg/kg)
(200 mg/kg) (200 mg/kg)
43 2000-0/4
50 25 38 51
44 .sup.Δ 1400
62.5 50 33
45 1000-2/4
50 12.5 125 59
2000-4/4
46 2000-0/4 25 84
(200 mg/kg) (200 mg/kg)
47 2000-0/4
75 62.5 19 27
48 2000-0/4
.sup.Δ 111(87-141)
.sup.Δ 110(75-162)
46
(200 mg/kg)
49 2000-0/4
50 .sup.Δ 50(29-83)
55 57
(40 mg/kg)
50 2000-0/4
62.5 25 27 47
51 2000-0/4
50 37.5 83 34
52 2000-0/4
62.5 37.5 38
53 2000-0/4
12.5 25 40
54 1000-0/4
50 12.5 39
2000-3/4
55 500-2/4
12.5 12.5 22
1000-3/4
56 2000-0/4
62.5 37.5 42
57 1000-0/4
100 50
2000-2/4
58 2000-0/4
37.5 37.5
59 1000-1/4
25 25
2000-4/4
60 2000-0/4
25 25
61 2000-0/4
50 12.5
62 1000-0/4 25
2000-1/4
63 1000-0/4
50 25 50
2000-4/4
64* 2000-0/4
37.5 12.5
(200 mg/kg)
__________________________________________________________________________
The followings are examples of preparation for analgesic, anti-pyretic or anti-inflammatory composition containing 1,3,5-substituted biuret compound of the formula (1) as the active ingredient.
______________________________________
Preparation 1
Ingredients Amount (mg)
______________________________________
1,3-Dimethyl-5-phenylbiuret
200
(Compound No. 3)
Lactose 500
Corn starch 280
Hydroxypropylcellulose
20
To make one package contains
1,000
______________________________________
By using the ingredients in the above-mentioned formulation, granular preparation is prepared by conventional methods.
______________________________________
Preparation 2
Ingredients Amount (mg)
______________________________________
1,3-Dimethyl-5-(4-methoxyphenyl)-
biuret (Compound No. 8)
100
Lactose 85
Crystalline cellulose
50
Hydroxypropylstarch 30
Talc 4
Magnesium stearate 1
To make one tablet contains
270
______________________________________
By using the ingredients in the above-mentioned formulation, tablet preparation is prepared by conventional methods.
______________________________________
Preparation 3
Ingredients Amount (mg)
______________________________________
1,3-Dimethyl-5-(3-pyridyl)-
biuret (Compound No. 15)
100
Lactose 50
Potate starch 50
Crystalline cellulose
109
Magnesium stearate 1
To make one capsule contains
310
______________________________________
By using the ingredients in the above-mentioned formulation, a capsule preparation is prepared by conventional methods.
______________________________________
Preparation 4
Ingredients Amounts (mg)
______________________________________
1-Ethyl-3-methyl-5-phenylbiuret
200
(Compound No. 31)
Lactose 100
Crystalline cellulose
98
Magnesium stearate 2
To make one capsule contains
400
______________________________________
By using the ingredients in the above-mentioned formulation, a capsule preparation is prepared by conventional methods.
______________________________________
Preparation 5
Ingredients Amounts (mg)
______________________________________
1-Ethyl-3-methyl-5-(3,4,5-
trimethoxyphenyl)biuret
250
(Compound No. 37)
Witepzol W-35 750
(A trade name for a suppository
base material manufactured by
and sold from Dynamite Nobel
Company.)
To make one suppository contains
1,000
______________________________________
By using the ingredients in the above-mentioned formulation, a suppository preparation is prepared by conventional methods.
______________________________________
Preparation 6
Ingredients Amounts (mg)
______________________________________
1-(2-Methyl-2-hydroxypropyl)-3-
methyl-5-phenylbiuret
100
(Compound No. 57)
Sodium chloride 16
Distilled water for injection
q.s.
To make one ampule contains
2 ml
______________________________________
By using the ingredients in the above-mentioned formulation, an injection preparation (ampule) is prepared by conventional methods.
______________________________________
Preparation 7
Ingredients Amount (g)
______________________________________
1-Ethyl-3-methyl-5-phenylbiuret
2.0
(Compound No. 31)
White vaserine 23.0
Stearyl alcohol 22.0
Propylene glycol 12.0
Sodium laurylsulfate 1.5
Ethyl p-oxybenzoate 0.025
Propyl p-oxybenzoate 0.015
Purified water q.s.
To make the whole 100
______________________________________
By using the ingredients in the above-mentioned formulation, an ointment preparation is prepared by conventional methods.
______________________________________
Preparation 8
Ingredients Amount (mg)
______________________________________
1-Methyl-3-ethyl-5-phenylbiuret
100
(Compound No. 21)
Lactose 85
Crystalline cellulose
50
Hydroxypropylstarch 30
Talc 4
Magnesium stearate 1
To make one tablet contains
270
______________________________________
By using the ingredients in the above-mentioned formulation, tablet preparation is prepared by conventional methods.
______________________________________
Preparation 9
Ingredients Amount (mg)
______________________________________
1-Ethyl-3-methyl-5-phenylbiuret
100
(Compound No. 31)
Lactose 50
Potate starch 50
Crystalline cellulose
109
Magnesium stearate 1
To make one capsule contains
310
______________________________________
By using the ingredients in the above-mentioned formulation, a capsule preparation is prepared by conventional methods.
______________________________________
Preparation 10
Ingredients Amounts (mg)
______________________________________
1-n-Propyl-3-methyl-5-phenylbiuret
200
(Compound No. 41)
Lactose 100
Crystalline cellulose
98
Magnesium stearate 2
To make one capsule contains
400
______________________________________
By using the ingredients in the above-mentioned formulation, a capsule preparation is prepared by conventional method.
______________________________________
Preparation 11
Ingredients Amounts (mg)
______________________________________
1-Isopropyl-3-methyl-5-phenylbiuret
250
(Compound No. 43)
Witepzol W-35 750
(A trade name for suppository base
material manufactured by and sold from
Dynamite Nobel Company)
To make one suppository contains
1,000
______________________________________
By using the ingredients in the above-mentioned formulation, a suppository preparation is prepared by conventional methods.
______________________________________
Preparation 12
Ingredients Amounts (mg)
______________________________________
1-Propenyl-3-methyl-5-phenylbiuret
100
(Compound No. 45)
Sodium chloride 16
Distilled water for injection
q.s.
To make one ampule contains
2 ml
______________________________________
By using the ingredients in the above-mentioned formulation, an injection preparation (ampule) is prepared by conventional methods.
______________________________________
Preparation 13
Ingredient Amount (g)
______________________________________
1-Isobutyl-3-methyl-5-phenylbiuret
2.0
(Compound No. 49)
White vaserine 23.0
Stearyl alcohol 22.0
Propylene glycol 12.0
Sodium laurylsulfate 1.5
Ethyl p-oxybenzoete 0.025
Propyl p-oxybenzoete 0.015
Purified water q.s.
To make the whole 100
______________________________________
By using the ingredients in the above-mentioned formulation, an ointment preparation is prepared by conventional methods.
Claims (7)
1. A method of treating a patient requiring analgesia, said method comprising administering to said patient an analgesic amount of a compound of the formula (1): ##STR80## wherein R1 is a hydrogen atom, a lower alkyl group, a substituted lower alkyl group having chlorine atom(s), cyano group(s), dimethylamino group(s), hydroxy group(s), methoxy group(s) or carboxy group(s) as the substituents, a lower alkenyl group, a hydroxy group, a methoxy group, an acetyl group or a phenyl group; R2 is a hydrogen atom, a lower alkyl group or a phenyl group; R3 is a pyridyl group, a substituted pyridyl group having methyl group(s) as the substituent(s) or a pyridyl methyl group.
2. A method of treating a patient having a pyretic or inflammatory condition, said method comprising administering to said patient a therapeutically effective amount of a compound of the formula: ##STR81## wherein R1 is a hydrogen atom, a lower alkyl group, a substituted lower alkyl group having chlorine atom(s), cyano group(s), dimethylamino group(s), hydroxy group(s), methoxy group(s) or carboxy group(s) as the substituents, a lower alkenyl group, a hydroxy group, a methoxy group, an acetyl group or a phenyl group; R2 is a hydrogen atom, a lower alkyl group or a phenyl group; R3 is a pyridyl group, a substituted pyridyl group having methyl group(s) as the substituent(s) or a pyridyl methyl group.
3. Method of claim 1 or claim 2, wherein said amount is from about 10 to about 2000 mg per day for an adult.
4. Method of claim 1 or claim 2, wherein said daily dosage amount is divided into 2 or 3 portions which are separately administered.
5. Method of claim 1 or claim 2, wherein said compound of the formula (1) is administered orally or topically or by injection or suppository.
6. An analgesic, anti-inflammatory or anti-pyretic composition containing as the active ingredient a 1,3,5-substituted biuret compound of the formula (1) ##STR82## wherein R1 is a hydrogen atom, a lower alkyl group, a substituted lower alkyl group having chlorine atom(s), cyano group(s), dimethylamino group(s), hydroxy group(s), methoxy group(s) or carboxy group(s), as the substituent(s), a lower alkenyl group, a hydroxy group, a methoxy group, an acetyl group or a phenyl group; R2 is a hydrogen atom, a lower alkyl group or a phenyl group; R3 is a pyridyl group, a substituted pyridyl group having methyl group(s) as the substituent(s) or a pyridyl methyl group.
7. Composition of claim 6, wherein said composition is in the form of a tablet, capsule, granules, powder, injection preparation, suppository preparation, topical ointment or cream or peroral syrup, elixir or oily suspension.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP54/38793 | 1979-03-31 | ||
| JP3879379A JPS55130912A (en) | 1979-03-31 | 1979-03-31 | Antiphlogistic agent |
| JP3879179A JPS55130910A (en) | 1979-03-31 | 1979-03-31 | Analgesic |
| JP54/38791 | 1979-03-31 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/134,411 Division US4287207A (en) | 1979-03-31 | 1980-03-27 | Pharmaceutical composition containing 1,3,5-substituted biuret compound |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4350700A true US4350700A (en) | 1982-09-21 |
Family
ID=26378076
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/134,411 Expired - Lifetime US4287207A (en) | 1979-03-31 | 1980-03-27 | Pharmaceutical composition containing 1,3,5-substituted biuret compound |
| US06/257,583 Expired - Lifetime US4350700A (en) | 1979-03-31 | 1981-04-27 | Pharmaceutical composition containing 1,3,5-substituted biuret compound |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/134,411 Expired - Lifetime US4287207A (en) | 1979-03-31 | 1980-03-27 | Pharmaceutical composition containing 1,3,5-substituted biuret compound |
Country Status (4)
| Country | Link |
|---|---|
| US (2) | US4287207A (en) |
| DE (1) | DE3012190C2 (en) |
| FR (1) | FR2452925A1 (en) |
| GB (1) | GB2055043B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114901280A (en) * | 2019-11-05 | 2022-08-12 | 德米拉公司 | MrgprX2 antagonists and uses thereof |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8529797D0 (en) * | 1985-12-03 | 1986-01-08 | Shell Int Research | Herbicides |
| US5153223A (en) * | 1991-04-24 | 1992-10-06 | Warner-Lambert Company | Biurets, aminocarbonyl carbamates, and aminocarbonyl thiocarbamates useful as ACAT inhibitors |
| WO2007082908A2 (en) * | 2006-01-20 | 2007-07-26 | L'oréal | Use of biuret derivatives for moisturizing the skin. |
| FR2896408B1 (en) * | 2006-01-20 | 2008-03-14 | Oreal | USE OF BIURET DERIVATIVES FOR MOISTURIZING THE SKIN |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB819853A (en) | 1956-12-21 | 1959-09-09 | Bayer Ag | Substituted urea herbicides |
| GB1096006A (en) | 1965-03-09 | 1967-12-20 | Horner Frank W Ltd | Substituted biurets |
-
1980
- 1980-03-27 US US06/134,411 patent/US4287207A/en not_active Expired - Lifetime
- 1980-03-28 DE DE3012190A patent/DE3012190C2/en not_active Expired
- 1980-03-28 FR FR8007036A patent/FR2452925A1/en active Granted
- 1980-03-31 GB GB8010753A patent/GB2055043B/en not_active Expired
-
1981
- 1981-04-27 US US06/257,583 patent/US4350700A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB819853A (en) | 1956-12-21 | 1959-09-09 | Bayer Ag | Substituted urea herbicides |
| GB1096006A (en) | 1965-03-09 | 1967-12-20 | Horner Frank W Ltd | Substituted biurets |
Non-Patent Citations (1)
| Title |
|---|
| J.A.C.S. Jun. (1940) 1595-1596. * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114901280A (en) * | 2019-11-05 | 2022-08-12 | 德米拉公司 | MrgprX2 antagonists and uses thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2452925B1 (en) | 1983-06-24 |
| US4287207A (en) | 1981-09-01 |
| DE3012190C2 (en) | 1985-09-26 |
| DE3012190A1 (en) | 1980-10-02 |
| GB2055043A (en) | 1981-02-25 |
| GB2055043B (en) | 1983-10-19 |
| FR2452925A1 (en) | 1980-10-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR100589868B1 (en) | Amide derivative | |
| US4340598A (en) | Hypotensive imidazole derivatives | |
| US6037377A (en) | Amidine derivatives, the preparation and use thereof as medicaments with LTB4 antagonistic effect | |
| Dogan et al. | Synthesis, structure elucidation and antimicrobial activity of some 3-hydroxy-2-naphthoic acid hydrazide derivatives | |
| US4252804A (en) | Therapeutically useful 3,4,5-trimethoxybenzene derivatives | |
| US5017596A (en) | Arylpyrazolylcarbinol compounds with analgesic activity | |
| JP3290998B2 (en) | Aminothiazole derivative, method for producing the same, and pharmaceutical composition containing the same | |
| US4002749A (en) | Substituted indolinones | |
| FR2501690A1 (en) | HETEROCYCLIC DERIVATIVES OF THE 1,2,4-TRIAZOLE TYPE, THEIR PREPARATION AND THEIR PHARMACOLOGICAL APPLICATION | |
| US4539322A (en) | Dihydropyridine derivatives and their use in treating heart conditions and hypertension | |
| US5453514A (en) | Pyrazole derivatives and compositions and methods of use as maillard reaction inhibitors | |
| EP1758852B1 (en) | Substituted cyclopentene compounds | |
| HU187478B (en) | Process for preparing new imidazolyl-phenyl-amidines and pharmaceutical compositions containing thereof | |
| US5342850A (en) | Thiazolidine-2,4-dione derivatives, their salts and their preparation processes | |
| GB2243832A (en) | 2-substituted 4-acetamido-5-chloro-n-[2-(diethylamino)ethyl]-benzamide derivative | |
| US5288758A (en) | New urea derivatives, their preparation and their application in therapy | |
| HU185647B (en) | Process for producing new 4h-1,2,4-triazole derivatives | |
| US5244894A (en) | 2-aminopyrimidine-4-carboxamide derivatives, their preparation and their use in therapeutics | |
| US4350700A (en) | Pharmaceutical composition containing 1,3,5-substituted biuret compound | |
| US4666911A (en) | Allophanoylpiperazine compound and analgesic composition containing same as active ingredient | |
| US4344948A (en) | Piperidine derivatives and pharmaceutical compositions containing same | |
| US4278672A (en) | Pharmaceutical composition and methods of use containing 1,1,3,5-substituted biuret compound | |
| US4616017A (en) | Aminohydroxypropoxy substituted aryl compounds | |
| US5084457A (en) | Benzoylaminoquinazolinones | |
| US4293713A (en) | Novel 1,1,3,5-substituted biuret compound and a pharmaceutical composition containing the same |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| STCF | Information on status: patent grant |
Free format text: PATENTED CASE |
|
| MAFP | Maintenance fee payment |
Free format text: PAYMENT OF MAINTENANCE FEE, 4TH YEAR, PL 96-517 (ORIGINAL EVENT CODE: M170); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY Year of fee payment: 4 |
|
| FEPP | Fee payment procedure |
Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY |
|
| MAFP | Maintenance fee payment |
Free format text: PAYMENT OF MAINTENANCE FEE, 8TH YEAR, PL 96-517 (ORIGINAL EVENT CODE: M171); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY Year of fee payment: 8 |
|
| FEPP | Fee payment procedure |
Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY Free format text: PAYER NUMBER DE-ASSIGNED (ORIGINAL EVENT CODE: RMPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY |
|
| MAFP | Maintenance fee payment |
Free format text: PAYMENT OF MAINTENANCE FEE, 12TH YEAR, LARGE ENTITY (ORIGINAL EVENT CODE: M185); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY Year of fee payment: 12 |
|
| FEPP | Fee payment procedure |
Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY Free format text: PAYER NUMBER DE-ASSIGNED (ORIGINAL EVENT CODE: RMPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY |